Variant report

Variant	rs147265683
Chromosome Location	chr7:103451140-103451141
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3365947	chr7:103451111-103451357	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103446200-103452000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr7:103449200-103451200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr7:103449200-103451200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr7:103449200-103451200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:103449200-103451200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:103449800-103451200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr7:103450000-103452200	Enhancers	Liver	Liver
8	chr7:103450200-103451600	Flanking Active TSS	K562	blood
9	chr7:103450200-103452800	Enhancers	Fetal Kidney	kidney
10	chr7:103450400-103451200	Flanking Active TSS	HepG2	liver
11	chr7:103450600-103451200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:103450600-103452400	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr7:103450800-103456600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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